South Korea showcases top 10 innovative medical devices at annual report meeting South Korea reveals its top ten groundbreaking healthcare technologies at a major annual event ...

RenovoRx's innovative RenovoCath and TAMP platform show promising clinical data. Click here to read why RNXT stock presents ...

The FDA’s framework for AI regulation, while robust for premarket evaluation, would benefit from more specific mechanisms for continuous monitoring of AI performance in diverse real-world settings.

The FDA alerts healthcare providers that certain patient monitors from Contec and Epsimed are gathering data and beaming it to a hardcoded IP address.

The FDA raised concerns about cybersecurity vulnerabilities in the patient monitors that could allow unauthorized individuals ...

By applying AI, the analysis can focus on biological changes ... received clearances from U.S. and European regulators as a medical device. At hospitals, clinicians can use the technology to ...

CHICAGO, Jan 24 (Reuters) - The U.S. Food and Drug Administration has pulled draft guidance from its website requiring companies to test medicines and devices in diverse populations as part of a ...

South Korea’s Ministry of Food and Drug Safety said it released the world’s first guideline on reviewing and approving generative artificial intelligence-based medical devices Jan. 24, to help ...

The Food and Drug Administration announced it would decide by April 2024 whether chemical hair straightening products sold in the U.S. would be banned from using formaldehyde or ingredients that ...

But with most users reporting only mild-to-moderate side-effects and the FDA’s approval, Spravato may offer a new option for the many Americans who have long struggled with drug-resistant ...